Chiu Ricky Y T, Thach Alison V, Wu Chloe M, Wu Benjamin M, Kamei Daniel T
Department of Bioengineering, University of California, Los Angeles, Los Angeles, California, United States of America.
Division of Advanced Prosthodontics & Weintraub Center for Reconstructive Biotechnology, UCLA School of Dentistry, Los Angeles, California, United States of America.
PLoS One. 2015 Nov 10;10(11):e0142654. doi: 10.1371/journal.pone.0142654. eCollection 2015.
The paper-based immunoassay for point-of-care diagnostics is widely used due to its low cost and portability over traditional lab-based assays. Lateral-flow immunoassay (LFA) is the most well-established paper-based assay since it is rapid and easy to use. However, the disadvantage of LFA is its lack of sensitivity in some cases where a large sample volume is required, limiting its use as a diagnostic tool. To improve the sensitivity of LFA, we previously reported on the concentration of analytes into one of the two bulk phases of an aqueous two-phase system (ATPS) prior to detection. In this study, we preserved the advantages of LFA while significantly improving upon our previous proof-of-concept studies by employing a novel approach of concentrating gold nanoparticles, a common LFA colorimetric indicator. By conjugating specific antibodies and polymers to the surfaces of the particles, these gold nanoprobes (GNPs) were able to capture target proteins in the sample and subsequently be concentrated within 10 min at the interface of an ATPS solution comprised of polyethylene glycol, potassium phosphate, and phosphate-buffered saline. These GNPs were then extracted and applied directly to LFA. By combining this prior ATPS interface extraction with LFA, the detection limit of LFA for a model protein was improved by 100-fold from 1 ng/μL to 0.01 ng/μL. Additionally, we examined the behavior of the ATPS system in fetal bovine serum and synthetic urine to more closely approach real-world applications. Despite using more complex matrices, ATPS interface extraction still improved the detection limit by 100-fold within 15 to 25 min, demonstrating the system's potential to be applied to patient samples.
基于纸的即时诊断免疫分析因其低成本和相对于传统实验室检测的便携性而被广泛使用。侧向流动免疫分析(LFA)是最成熟的基于纸的检测方法,因为它快速且易于使用。然而,LFA的缺点是在某些需要大量样本的情况下缺乏灵敏度,限制了其作为诊断工具的应用。为了提高LFA的灵敏度,我们之前报道了在检测前将分析物浓缩到水两相系统(ATPS)的两个本体相之一中。在本研究中,我们保留了LFA的优点,同时通过采用一种浓缩金纳米颗粒(一种常见的LFA比色指示剂)的新方法,显著改进了我们之前的概念验证研究。通过将特异性抗体和聚合物缀合到颗粒表面,这些金纳米探针(GNP)能够捕获样品中的目标蛋白质,并随后在由聚乙二醇、磷酸钾和磷酸盐缓冲盐水组成的ATPS溶液界面处10分钟内被浓缩。然后提取这些GNP并直接应用于LFA。通过将这种先前的ATPS界面提取与LFA相结合,LFA对模型蛋白的检测限从1 ng/μL提高到0.01 ng/μL,提高了100倍。此外,我们在胎牛血清和合成尿液中研究了ATPS系统的行为,以更接近实际应用。尽管使用了更复杂的基质,ATPS界面提取仍在15至25分钟内将检测限提高了100倍,证明了该系统应用于患者样本的潜力。